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The form collects protocol essentials such as protocol title, principal investigator details, submission or revision date, and clear study objectives. It requires background and rationale supported by literature, resource and staff qualifications, subject population eligibility criteria and accrual totals, and detailed study procedures including instruments, record sources, privacy protections, and an overall timeline. Additional sections address foreseeable risks, risk-minimization measures, and expected participant benefits, alongside recruitment methods and consent procedures.","RESEARCH REQUEST\nTemplate for Requesting Permission to Conduct Research at MSU Denver\nPlease complete this form.\nAs you are writing your RESEARCH REQUEST, remove all text in blue italics (and re-set the font color to black), so this guidance is not contained in the final version of your document.\nDo not use this template like a form where you are answering questions or responding to guidance cues.  Use complete sentences and describe all processes and procedures thoroughly. When you remove the instructions/guidance, your RESEARCH REQUEST needs to make sense.\nPROTOCOL TITLE:\nInclude the full protocol title.\nPRINCIPAL INVESTIGATOR:\nName, Department, Telephone Number, Email Address\nDATE:\nInclude the date of submission or revision.\nObjectives\nDescribe the purpose, specific aims, or objectives of the study.\nBackground\nDescribe the relevant prior experience and gaps in current knowledge.\nDescribe any relevant preliminary data.\nProvide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how it will add to existing knowledge.\nDescribe the resources available to accomplish this research.  Specifically include a summary of the qualifications (e.g., training, experience, oversight) of you and your staff as required to perform their role.  When applicable describe your knowledge of the local study sites, culture, language, and society.\nSubject Population\nDescribe the eligibility criteria that define who will be included and/or excluded in your study sample.  Please specify whether you intend to collect data from MSU Denver students, staff, administration, or if you intend to use de-identified aggregated Institutional Research Data.\nIf you will include or exclude any of the following special populations, this should be clearly stated: adults unable to consent; children (\u003C 18 years of age); pregnant women.\nClearly state the total number of subjects to be accrued in this study.  If this study is part of a larger multi-site project, clarify the total number of subjects to be accrued locally.\nProcedures Involved\nDescribe and explain the study design.\nProvide a description of all research procedures being performed and how, when, and where they are performed. Use bullet points or simple step-by-step language to describe procedures in the order in which they will occur.\nInclude, when applicable:\nA list and description of all study instruments and/or data that will be collected (e.g., surveys, questionnaires, demographic questions, interview questions, data collection forms, observations, recordings, etc.).  Study instruments should be referenced here and uploaded into IRBNet as separate documents.\nIf data will be collected via audio-taping, video-taping, or photography, this should be specified.\nExpected time commitment for participants (per specific procedure or task and in total).\nA description of any source records that will be used to collect data about subjects (e.g., student educational records, medical records, online resources, etc.).  For record reviews, specify the date range for the collection of data.\nA description of the setting, sites, and/or locations where your research team will conduct the research.\nAny provisions to protect the privacy interests of subjects. “Privacy interest” refers to a person’s desire to place limits on whom they interact or whom they provide personal information. (Example of a privacy protection: Conducting interviews in a quiet setting where others cannot overhear the conversation.)\nAn overall timeline for the research.\nRisks to Subjects\nList the reasonably foreseeable risks, discomforts, hazards, or inconveniences to the subjects related the subjects’ participation in the research. Consider physical, psychological, social, legal, and economic risks. Acknowledge any burden of time, inconvenience, etc.\nDescribe any plans or measures that will be taken to minimize risks, discomforts, hazards, and/or inconveniences related the subje","cbCaiiCpI27O7ckE","https://ap.wps.com/l/cbCaiiCpI27O7ckE","docx",19521,4,"English","en",105,"# Research Request Template\n## Protocol and Submission Details\n## Objectives and Background\n## Subject Population\n## Procedures Involved\n## Risks to Subjects\n## Potential Benefits to Subjects\n## Recruitment Methods\n## Consent Process","[{\"question\":\"What information must be included in the research request header?\",\"answer\":\"Include the full protocol title, the principal investigator’s name, department, telephone number, and email address, and the submission or revision date.\"},{\"question\":\"How should the study’s background and significance be written?\",\"answer\":\"Describe relevant prior experience and knowledge gaps, any preliminary data, and provide a scholarly rationale and significance based on existing literature and how the study adds to current knowledge.\"},{\"question\":\"What must be detailed in the recruitment and consent sections?\",\"answer\":\"Recruitment Methods should specify how eligible subjects will be identified, when/where/how recruitment occurs, and all recruitment materials. 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